Crescenzo Francesco, Danese Alessandra, Dall'Ora Francesco, Turazzini Michelangelo
Neurology Unit, Mater Salutis Hospital, AULSS 9 Scaligera, 37045 Legnago, Italy.
Neurology B Unit, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, 37124 Verona, Italy.
Int J Mol Sci. 2025 Mar 4;26(5):2289. doi: 10.3390/ijms26052289.
Chronic graft-versus-host disease (cGVHD) is a prognostically negative event following hematopoietic stem cell transplant (HSCT). While cGVHD mainly affects the muscles, skin, oral mucosa, eyes, lungs, gastrointestinal tract, and liver, central nervous system (CNS) involvement remains possible and, moreover, is rare when it occurs isolated. CNS-cGVHD can manifest with a wide spectrum of CNS disorders, including cerebrovascular diseases, autoimmune demyelinating diseases, and immune-mediated encephalitis. We present a case of 65-year-old man previously treated with HSCT presenting with progressive cerebrovascular disorder and optic neuropathy without any clear alternative causal processes except for immune-mediated CNS microangiopathy in the context of possible CNS-cGVHD, along with suggestive imaging and instrumental and laboratory findings. Starting one year after HSCT for acute myeloid leukemia, when the first cerebral ischemic event occurred and was then associated with a reduction in visual acuity, an extensive diagnostic work-up had remained inconclusive over many years, leading us to the hypothesis of CNS-cGVHD and, therefore, to the start of immunosuppressive therapy. Our experience highlighted not ignoring the possibility of cGVHD as the underlying mechanism of CNS disorder, even in the absence of other systemic presentations, once more common etiologies of CNS pathological processes have been ruled out.
慢性移植物抗宿主病(cGVHD)是造血干细胞移植(HSCT)后预后不良的事件。虽然cGVHD主要影响肌肉、皮肤、口腔黏膜、眼睛、肺、胃肠道和肝脏,但中枢神经系统(CNS)受累仍有可能,而且单独发生时很罕见。CNS-cGVHD可表现为多种中枢神经系统疾病,包括脑血管疾病、自身免疫性脱髓鞘疾病和免疫介导的脑炎。我们报告一例65岁男性患者,此前接受过HSCT治疗,出现进行性脑血管疾病和视神经病变,除了在可能的CNS-cGVHD背景下的免疫介导的中枢神经系统微血管病外,没有任何明确的其他因果过程,同时伴有提示性的影像学、仪器检查和实验室检查结果。在因急性髓系白血病接受HSCT一年后,首次发生脑缺血事件,随后视力下降,多年来广泛的诊断检查仍无定论,这使我们提出CNS-cGVHD的假设,因此开始免疫抑制治疗。我们的经验强调,即使没有其他全身表现,一旦排除了中枢神经系统病理过程更常见的病因,也不能忽视cGVHD作为中枢神经系统疾病潜在机制的可能性。